NP-MRD: Showing NP-Card for tonkinochromane L (NP0037946)

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Record Information

Version

2.0

Created at

2021-06-20 20:45:25 UTC

Updated at

2021-06-30 00:10:27 UTC

NP-MRD ID

NP0037946

Secondary Accession Numbers

None

Natural Product Identification

Common Name

tonkinochromane L

Provided By

JEOL Database JEOL Logo

Description

tonkinochromane L is found in Sophora tonkinensis. tonkinochromane L was first documented in 2008 (Li, X.-N., et al.).

Structure

MOL 3D MOL SDF 3D SDF PDB SMILES InChI


  Mrv1652306202122453D          

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M  END

     RDKit          3D

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  Mrv1652306202122453D          

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  7  8  1  0  0  0  0
  8 10  1  0  0  0  0
 15 16  1  0  0  0  0
 10 11  1  0  0  0  0
  5  6  1  0  0  0  0
  7 19  2  0  0  0  0
  2  1  1  0  0  0  0
 21 41  1  0  0  0  0
 21 42  1  0  0  0  0
 10 31  1  0  0  0  0
 10 32  1  0  0  0  0
 11 33  1  0  0  0  0
 11 34  1  0  0  0  0
 19 40  1  0  0  0  0
  4 29  1  0  0  0  0
 18 39  1  0  0  0  0
 14 36  1  0  0  0  0
 13 35  1  0  0  0  0
 22 43  1  0  0  0  0
 24 44  1  0  0  0  0
 24 45  1  0  0  0  0
 24 46  1  0  0  0  0
 25 47  1  0  0  0  0
 25 48  1  0  0  0  0
 25 49  1  0  0  0  0
 17 38  1  0  0  0  0
 16 37  1  0  0  0  0
  6 30  1  0  0  0  0
  1 26  1  0  0  0  0
  1 27  1  0  0  0  0
  1 28  1  0  0  0  0
M  END
> <DATABASE_ID>
NP0037946

> <DATABASE_NAME>
NP-MRD

> <SMILES>
[H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C(=O)C1=C([H])C(=C(OC([H])([H])[H])C([H])=C1O[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

> <INCHI_IDENTIFIER>
InChI=1S/C21H24O4/c1-14(2)4-8-16-12-18(20(24)13-21(16)25-3)19(23)11-7-15-5-9-17(22)10-6-15/h4-6,9-10,12-13,22,24H,7-8,11H2,1-3H3

> <INCHI_KEY>
APTIMVGBTQSTFO-UHFFFAOYSA-N

> <FORMULA>
C21H24O4

> <MOLECULAR_WEIGHT>
340.419

> <EXACT_MASS>
340.167459253

> <JCHEM_ACCEPTOR_COUNT>
4

> <JCHEM_ATOM_COUNT>
49

> <JCHEM_AVERAGE_POLARIZABILITY>
37.778237327947636

> <JCHEM_BIOAVAILABILITY>
1

> <JCHEM_DONOR_COUNT>
2

> <JCHEM_FORMAL_CHARGE>
0

> <JCHEM_GHOSE_FILTER>
1

> <JCHEM_IUPAC>
1-[2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-3-(4-hydroxyphenyl)propan-1-one

> <ALOGPS_LOGP>
4.15

> <JCHEM_LOGP>
5.423566909666667

> <ALOGPS_LOGS>
-4.98

> <JCHEM_MDDR_LIKE_RULE>
0

> <JCHEM_NUMBER_OF_RINGS>
2

> <JCHEM_PHYSIOLOGICAL_CHARGE>
0

> <JCHEM_PKA>
9.625208848953203

> <JCHEM_PKA_STRONGEST_ACIDIC>
8.887806781814161

> <JCHEM_PKA_STRONGEST_BASIC>
-4.858103957974512

> <JCHEM_POLAR_SURFACE_AREA>
66.76

> <JCHEM_REFRACTIVITY>
100.45150000000001

> <JCHEM_ROTATABLE_BOND_COUNT>
7

> <JCHEM_RULE_OF_FIVE>
0

> <ALOGPS_SOLUBILITY>
3.54e-03 g/l

> <JCHEM_TRADITIONAL_IUPAC>
1-[2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-3-(4-hydroxyphenyl)propan-1-one

> <JCHEM_VEBER_RULE>
0

$$$$

     RDKit          3D

 49 50  0  0  0  0  0  0  0  0999 V2000
    0.9040   -5.7401    3.9758 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6966   -4.3740    3.6385 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3492   -4.0887    2.3447 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2259   -5.0397    1.3292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1431   -4.6529    0.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2170   -5.6635   -0.8860 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4187   -3.3134   -0.2667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8307   -2.9438   -1.6539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6453   -3.7657   -2.5564 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4818   -1.6072   -1.9506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5623   -0.7095   -2.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5529   -0.1136   -1.9513 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7994   -0.7519   -1.8738 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8141   -0.2298   -1.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5821    0.9349   -0.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5417    1.4759    0.4575 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3571    1.5860   -0.4178 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3413    1.0627   -1.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2787   -2.3611    0.7468 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1125   -2.7335    2.0505 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2407   -1.6480    3.1016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1014   -1.2319    3.6436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7369   -0.0525    3.4934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2186    1.1227    2.7119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0834    0.1758    4.1302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0053   -6.3292    3.8177 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1488   -5.7868    5.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7507   -6.1586    3.4219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4134   -6.0940    1.5028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3744   -5.2534   -1.7669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8423   -1.1116   -1.0457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3827   -1.8328   -2.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1379   -1.2596   -3.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1512    0.1070   -3.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9849   -1.6666   -2.4345 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7686   -0.7442   -1.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3401    0.9259    0.3980 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1932    2.4974    0.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6160    1.5771   -1.2623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4503   -1.3059    0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7979   -0.8106    2.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8633   -1.9844    3.9389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5839   -2.0082    4.2388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2489    0.9433    2.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9206    1.3800    1.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1105    1.9925    3.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0349    1.0192    4.8267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8320    0.3997    3.3632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4331   -0.6979    4.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  2  0
 18 17  2  0
 15 14  2  0
 14 13  1  0
 11 12  1  0
  8  9  2  0
  7  5  1  0
  3  2  1  0
 20 21  1  0
 19 20  1  0
 21 22  1  0
 20  3  2  0
 22 23  2  3
  3  4  1  0
 23 24  1  0
  4  5  2  0
 23 25  1  0
 15 17  1  0
 12 18  1  0
  7  8  1  0
  8 10  1  0
 15 16  1  0
 10 11  1  0
  5  6  1  0
  7 19  2  0
  2  1  1  0
 21 41  1  0
 21 42  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 19 40  1  0
  4 29  1  0
 18 39  1  0
 14 36  1  0
 13 35  1  0
 22 43  1  0
 24 44  1  0
 24 45  1  0
 24 46  1  0
 25 47  1  0
 25 48  1  0
 25 49  1  0
 17 38  1  0
 16 37  1  0
  6 30  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
M  END

HEADER    PROTEIN                                 20-JUN-21   NONE
TITLE     NULL                                                        
COMPND    NULL                                                        
SOURCE    NULL                                                        
KEYWDS    NULL                                                        
EXPDTA    NULL                                                        
AUTHOR    Marvin                                                      
REVDAT   1   20-JUN-21         0                                  
HETATM    1  C   UNK     0       0.904  -5.740   3.976  0.00  0.00           C+0
HETATM    2  O   UNK     0       0.697  -4.374   3.639  0.00  0.00           O+0
HETATM    3  C   UNK     0       0.349  -4.089   2.345  0.00  0.00           C+0
HETATM    4  C   UNK     0       0.226  -5.040   1.329  0.00  0.00           C+0
HETATM    5  C   UNK     0      -0.143  -4.653   0.039  0.00  0.00           C+0
HETATM    6  O   UNK     0      -0.217  -5.664  -0.886  0.00  0.00           O+0
HETATM    7  C   UNK     0      -0.419  -3.313  -0.267  0.00  0.00           C+0
HETATM    8  C   UNK     0      -0.831  -2.944  -1.654  0.00  0.00           C+0
HETATM    9  O   UNK     0      -0.645  -3.766  -2.556  0.00  0.00           O+0
HETATM   10  C   UNK     0      -1.482  -1.607  -1.951  0.00  0.00           C+0
HETATM   11  C   UNK     0      -0.562  -0.710  -2.775  0.00  0.00           C+0
HETATM   12  C   UNK     0       0.553  -0.114  -1.951  0.00  0.00           C+0
HETATM   13  C   UNK     0       1.799  -0.752  -1.874  0.00  0.00           C+0
HETATM   14  C   UNK     0       2.814  -0.230  -1.069  0.00  0.00           C+0
HETATM   15  C   UNK     0       2.582   0.935  -0.346  0.00  0.00           C+0
HETATM   16  O   UNK     0       3.542   1.476   0.458  0.00  0.00           O+0
HETATM   17  C   UNK     0       1.357   1.586  -0.418  0.00  0.00           C+0
HETATM   18  C   UNK     0       0.341   1.063  -1.218  0.00  0.00           C+0
HETATM   19  C   UNK     0      -0.279  -2.361   0.747  0.00  0.00           C+0
HETATM   20  C   UNK     0       0.113  -2.733   2.050  0.00  0.00           C+0
HETATM   21  C   UNK     0       0.241  -1.648   3.102  0.00  0.00           C+0
HETATM   22  C   UNK     0      -1.101  -1.232   3.644  0.00  0.00           C+0
HETATM   23  C   UNK     0      -1.737  -0.053   3.493  0.00  0.00           C+0
HETATM   24  C   UNK     0      -1.219   1.123   2.712  0.00  0.00           C+0
HETATM   25  C   UNK     0      -3.083   0.176   4.130  0.00  0.00           C+0
HETATM   26  H   UNK     0      -0.005  -6.329   3.818  0.00  0.00           H+0
HETATM   27  H   UNK     0       1.149  -5.787   5.041  0.00  0.00           H+0
HETATM   28  H   UNK     0       1.751  -6.159   3.422  0.00  0.00           H+0
HETATM   29  H   UNK     0       0.413  -6.094   1.503  0.00  0.00           H+0
HETATM   30  H   UNK     0      -0.374  -5.253  -1.767  0.00  0.00           H+0
HETATM   31  H   UNK     0      -1.842  -1.112  -1.046  0.00  0.00           H+0
HETATM   32  H   UNK     0      -2.383  -1.833  -2.536  0.00  0.00           H+0
HETATM   33  H   UNK     0      -0.138  -1.260  -3.625  0.00  0.00           H+0
HETATM   34  H   UNK     0      -1.151   0.107  -3.212  0.00  0.00           H+0
HETATM   35  H   UNK     0       1.985  -1.667  -2.434  0.00  0.00           H+0
HETATM   36  H   UNK     0       3.769  -0.744  -1.019  0.00  0.00           H+0
HETATM   37  H   UNK     0       4.340   0.926   0.398  0.00  0.00           H+0
HETATM   38  H   UNK     0       1.193   2.497   0.150  0.00  0.00           H+0
HETATM   39  H   UNK     0      -0.616   1.577  -1.262  0.00  0.00           H+0
HETATM   40  H   UNK     0      -0.450  -1.306   0.556  0.00  0.00           H+0
HETATM   41  H   UNK     0       0.798  -0.811   2.670  0.00  0.00           H+0
HETATM   42  H   UNK     0       0.863  -1.984   3.939  0.00  0.00           H+0
HETATM   43  H   UNK     0      -1.584  -2.008   4.239  0.00  0.00           H+0
HETATM   44  H   UNK     0      -0.249   0.943   2.245  0.00  0.00           H+0
HETATM   45  H   UNK     0      -1.921   1.380   1.912  0.00  0.00           H+0
HETATM   46  H   UNK     0      -1.111   1.992   3.368  0.00  0.00           H+0
HETATM   47  H   UNK     0      -3.035   1.019   4.827  0.00  0.00           H+0
HETATM   48  H   UNK     0      -3.832   0.400   3.363  0.00  0.00           H+0
HETATM   49  H   UNK     0      -3.433  -0.698   4.690  0.00  0.00           H+0
CONECT    1    2   26   27   28                                             
CONECT    2    3    1                                                       
CONECT    3    2   20    4                                                  
CONECT    4    3    5   29                                                  
CONECT    5    7    4    6                                                  
CONECT    6    5   30                                                       
CONECT    7    5    8   19                                                  
CONECT    8    9    7   10                                                  
CONECT    9    8                                                            
CONECT   10    8   11   31   32                                             
CONECT   11   12   10   33   34                                             
CONECT   12   13   11   18                                                  
CONECT   13   12   14   35                                                  
CONECT   14   15   13   36                                                  
CONECT   15   14   17   16                                                  
CONECT   16   15   37                                                       
CONECT   17   18   15   38                                                  
CONECT   18   17   12   39                                                  
CONECT   19   20    7   40                                                  
CONECT   20   21   19    3                                                  
CONECT   21   20   22   41   42                                             
CONECT   22   21   23   43                                                  
CONECT   23   22   24   25                                                  
CONECT   24   23   44   45   46                                             
CONECT   25   23   47   48   49                                             
CONECT   26    1                                                            
CONECT   27    1                                                            
CONECT   28    1                                                            
CONECT   29    4                                                            
CONECT   30    6                                                            
CONECT   31   10                                                            
CONECT   32   10                                                            
CONECT   33   11                                                            
CONECT   34   11                                                            
CONECT   35   13                                                            
CONECT   36   14                                                            
CONECT   37   16                                                            
CONECT   38   17                                                            
CONECT   39   18                                                            
CONECT   40   19                                                            
CONECT   41   21                                                            
CONECT   42   21                                                            
CONECT   43   22                                                            
CONECT   44   24                                                            
CONECT   45   24                                                            
CONECT   46   24                                                            
CONECT   47   25                                                            
CONECT   48   25                                                            
CONECT   49   25                                                            
MASTER        0    0    0    0    0    0    0    0   49    0  100    0
END

RDKit          3D

49 50  0  0  0  0  0  0  0  0999 V2000
    0.9040   -5.7401    3.9758 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.6966   -4.3740    3.6385 O   0  0  0  0  0  0  0  0  0  0  0  0
    0.3492   -4.0887    2.3447 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2259   -5.0397    1.3292 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1431   -4.6529    0.0392 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2170   -5.6635   -0.8860 O   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4187   -3.3134   -0.2667 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.8307   -2.9438   -1.6539 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6453   -3.7657   -2.5564 O   0  0  0  0  0  0  0  0  0  0  0  0
   -1.4818   -1.6072   -1.9506 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.5623   -0.7095   -2.7753 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.5529   -0.1136   -1.9513 C   0  0  0  0  0  0  0  0  0  0  0  0
    1.7994   -0.7519   -1.8738 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.8141   -0.2298   -1.0690 C   0  0  0  0  0  0  0  0  0  0  0  0
    2.5821    0.9349   -0.3456 C   0  0  0  0  0  0  0  0  0  0  0  0
    3.5417    1.4759    0.4575 O   0  0  0  0  0  0  0  0  0  0  0  0
    1.3571    1.5860   -0.4178 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.3413    1.0627   -1.2181 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2787   -2.3611    0.7468 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.1125   -2.7335    2.0505 C   0  0  0  0  0  0  0  0  0  0  0  0
    0.2407   -1.6480    3.1016 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1014   -1.2319    3.6436 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.7369   -0.0525    3.4934 C   0  0  0  0  0  0  0  0  0  0  0  0
   -1.2186    1.1227    2.7119 C   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0834    0.1758    4.1302 C   0  0  0  0  0  0  0  0  0  0  0  0
   -0.0053   -6.3292    3.8177 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1488   -5.7868    5.0413 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.7507   -6.1586    3.4219 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.4134   -6.0940    1.5028 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.3744   -5.2534   -1.7669 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.8423   -1.1116   -1.0457 H   0  0  0  0  0  0  0  0  0  0  0  0
   -2.3827   -1.8328   -2.5359 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.1379   -1.2596   -3.6247 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1512    0.1070   -3.2122 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.9849   -1.6666   -2.4345 H   0  0  0  0  0  0  0  0  0  0  0  0
    3.7686   -0.7442   -1.0191 H   0  0  0  0  0  0  0  0  0  0  0  0
    4.3401    0.9259    0.3980 H   0  0  0  0  0  0  0  0  0  0  0  0
    1.1932    2.4974    0.1502 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.6160    1.5771   -1.2623 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.4503   -1.3059    0.5561 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.7979   -0.8106    2.6696 H   0  0  0  0  0  0  0  0  0  0  0  0
    0.8633   -1.9844    3.9389 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.5839   -2.0082    4.2388 H   0  0  0  0  0  0  0  0  0  0  0  0
   -0.2489    0.9433    2.2454 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.9206    1.3800    1.9116 H   0  0  0  0  0  0  0  0  0  0  0  0
   -1.1105    1.9925    3.3684 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.0349    1.0192    4.8267 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.8320    0.3997    3.3632 H   0  0  0  0  0  0  0  0  0  0  0  0
   -3.4331   -0.6979    4.6902 H   0  0  0  0  0  0  0  0  0  0  0  0
 12 13  2  0
 18 17  2  0
 15 14  2  0
 14 13  1  0
 11 12  1  0
  8  9  2  0
  7  5  1  0
  3  2  1  0
 20 21  1  0
 19 20  1  0
 21 22  1  0
 20  3  2  0
 22 23  2  3
  3  4  1  0
 23 24  1  0
  4  5  2  0
 23 25  1  0
 15 17  1  0
 12 18  1  0
  7  8  1  0
  8 10  1  0
 15 16  1  0
 10 11  1  0
  5  6  1  0
  7 19  2  0
  2  1  1  0
 21 41  1  0
 21 42  1  0
 10 31  1  0
 10 32  1  0
 11 33  1  0
 11 34  1  0
 19 40  1  0
  4 29  1  0
 18 39  1  0
 14 36  1  0
 13 35  1  0
 22 43  1  0
 24 44  1  0
 24 45  1  0
 24 46  1  0
 25 47  1  0
 25 48  1  0
 25 49  1  0
 17 38  1  0
 16 37  1  0
  6 30  1  0
  1 26  1  0
  1 27  1  0
  1 28  1  0
M  END

View in JSmol

Synonyms

Not Available

Chemical Formula

C₂₁H₂₄O₄

Average Mass

340.4190 Da

Monoisotopic Mass

340.16746 Da

IUPAC Name

1-[2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-3-(4-hydroxyphenyl)propan-1-one

Traditional Name

1-[2-hydroxy-4-methoxy-5-(3-methylbut-2-en-1-yl)phenyl]-3-(4-hydroxyphenyl)propan-1-one

CAS Registry Number

Not Available

SMILES

[H]OC1=C([H])C([H])=C(C([H])=C1[H])C([H])([H])C([H])([H])C(=O)C1=C([H])C(=C(OC([H])([H])[H])C([H])=C1O[H])C([H])([H])C([H])=C(C([H])([H])[H])C([H])([H])[H]

InChI Identifier

InChI=1S/C21H24O4/c1-14(2)4-8-16-12-18(20(24)13-21(16)25-3)19(23)11-7-15-5-9-17(22)10-6-15/h4-6,9-10,12-13,22,24H,7-8,11H2,1-3H3

InChI Key

APTIMVGBTQSTFO-UHFFFAOYSA-N

Experimental Spectra

Spectrum Type	Description	Depositor Email	Depositor Organization	Depositor	Deposition Date	View
1D NMR	¹³C NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 400 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 100 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 200 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 300 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 500 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 600 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 700 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 800 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 900 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹³C NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum
1D NMR	¹H NMR Spectrum (1D, 1000 MHz, acetone-d6, simulated)	Wishart Lab	Wishart Lab	David Wishart	2021-06-20	View Spectrum

Predicted Spectra

Not Available

Chemical Shift Submissions

Not Available

Species

Species of Origin

Species Name	Source	Reference
Sophora tonkinensis	JEOL database	Li, X.-N., et al, Phytochem. Letts. 1, 163 (2008)

Chemical Taxonomy

Classification

Not classified

Physical Properties

State

Not Available

Experimental Properties

Property	Value	Reference
Melting Point	Not Available	Not Available
Boiling Point	Not Available	Not Available
Water Solubility	Not Available	Not Available
LogP	Not Available	Not Available

Predicted Properties

Property	Value	Source
logP	4.15	ALOGPS
logP	5.42	ChemAxon
logS	-5	ALOGPS
pKa (Strongest Acidic)	8.89	ChemAxon
pKa (Strongest Basic)	-4.9	ChemAxon
Physiological Charge	0	ChemAxon
Hydrogen Acceptor Count	4	ChemAxon
Hydrogen Donor Count	2	ChemAxon
Polar Surface Area	66.76 Å²	ChemAxon
Rotatable Bond Count	7	ChemAxon
Refractivity	100.45 m³·mol⁻¹	ChemAxon
Polarizability	37.78 Å³	ChemAxon
Number of Rings	2	ChemAxon
Bioavailability	Yes	ChemAxon
Rule of Five	No	ChemAxon
Ghose Filter	Yes	ChemAxon
Veber's Rule	No	ChemAxon
MDDR-like Rule	No	ChemAxon

External Links

Not Available

References

General References

Li, X.-N., et al. (2008). Li, X.-N., et al, Phytochem. Letts. 1, 163 (2008). Phytochem..

Showing NP-Card for tonkinochromane L (NP0037946)

MOL for NP0037946 (tonkinochromane L)

3D MOL for NP0037946 (tonkinochromane L)

3D SDF for NP0037946 (tonkinochromane L)

3D-SDF for NP0037946 (tonkinochromane L)

PDB for NP0037946 (tonkinochromane L)

3D PDB for NP0037946 (tonkinochromane L)

SMILES for NP0037946 (tonkinochromane L)

INCHI for NP0037946 (tonkinochromane L)

Structure for NP0037946 (tonkinochromane L)

3D Structure for NP0037946 (tonkinochromane L)